HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21552Erstellt: 25. Oktober 2026
Benzyl Bromide → cis-4-Benzyloxy-2-buten-1-ol
https://huagongshe.com/reaction/21552
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | 2-Butene-1,4-diol, (2Z)- | HCID 643790 | — |
| Produkt | cis-4-Benzyloxy-2-buten-1-ol | HCID 11008492 | 63,2% |
Reaktionsschritte
14.6 g of sodium hydride (60 % in oil) was washed with n-pentane under an argon gas. After drying, 150 ml of dry dimethylformamide (hereinafter referred to simply as DMF) was added thereto to form a suspension. 75 g of (Z)-2-buten-1,4-diol was dropwise added thereto at 0° C. under stirring over a period of 30 minutes. The mixture was stirred at room temperature for 1.5 hours, and 44 g of benzyl bromide was added at 0° C. under stirring. The mixture was stirred at the same temperature for 30 minutes, and then the temperature was returned to room temperature. The mixture was stirred at 50° C. overnight. The reaction solution was poured into ice water and extracted with diethyl ether. The ether solution was washed sequentially with water and with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to distillation under reduced pressure (2.5 mmHg, 134°-138° C.) to obtain 29 g of (Z)-4-benzyloxy-2-buten-1-ol as colorless oily substance.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05424309 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-9186667cd3574337a99d237bd0b87c24 |
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| Quellennotiz | uspto-grants-1995_06 |
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